Philp Ashleigh M, Davis Edward T, Jones Simon W
Institute of Inflammation and Ageing, MRC-ARUK Centre for Musculoskeletal Ageing Research, Medical School, Queen Elizabeth Hospital, University of Birmingham.
The Royal Orthopaedic Hospital NHS Foundation Trust, Bristol Road South, Northfield, Birmingham.
Rheumatology (Oxford). 2017 Jun 1;56(6):869-881. doi: 10.1093/rheumatology/kew278.
OA is the most common joint disorder in the world, but there are no approved therapeutics to prevent disease progression. Historically, OA has been considered a wear-and-tear joint disease, and efforts to identify and develop disease-modifying therapeutics have predominantly focused on direct inhibition of cartilage degeneration. However, there is now increasing evidence that inflammation is a key mediator of OA joint pathology, and also that the link between obesity and OA is not solely due to excessive load-bearing, suggesting therefore that targeting inflammation in OA could be a rewarding therapeutic strategy. In this review we therefore re-evaluate historical clinical trial data on anti-inflammatory therapeutics in OA patients, highlight some of the more promising emerging therapeutic targets and discuss the implications for future clinical trial design.
骨关节炎是全球最常见的关节疾病,但目前尚无经批准可预防疾病进展的治疗方法。从历史上看,骨关节炎一直被视为一种磨损性关节疾病,识别和开发改善病情的治疗方法的努力主要集中在直接抑制软骨退变上。然而,现在越来越多的证据表明,炎症是骨关节炎关节病理的关键介质,而且肥胖与骨关节炎之间的联系并不完全是由于过度负重,因此表明针对骨关节炎中的炎症可能是一种有效的治疗策略。因此,在本综述中,我们重新评估了骨关节炎患者抗炎治疗的历史临床试验数据,突出了一些更有前景的新兴治疗靶点,并讨论了对未来临床试验设计的影响。